Jonas Ghouse

Novo Nordisk A/S, Novo Nordisk Park 1
Malov, 2760, Denmark

Last Updated: 09/26/2026

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Found 62 publications

Resistant Hypertension Variants Link to Hyperaldosteronism and Potassium Levels.

Resistant Hypertension Variants Link to Hyperaldosteronism and Potassium Levels.

Journal: Hypertension (Dallas, Tex. : 1979)

Published: July 09, 2026

Association between IL-6 and hs-CRP and Cardiovascular Risk in Clinically Relevant Subgroups.

Association between IL-6 and hs-CRP and Cardiovascular Risk in Clinically Relevant Subgroups.

Journal: European journal of preventive cardiology

Published: January 04, 2026

Fibrotic disease co-occurrence and associated risk of subsequent organ failure: a nationwide matched cohort study.

Fibrotic disease co-occurrence and associated risk of subsequent organ failure: a nationwide matched cohort study.

Journal: Rheumatology (Oxford, England)

Published: December 03, 2025

Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways.

Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways.

Journal: medRxiv : the preprint server for health sciences

Published: September 26, 2025

Plasma proteomic signature of the human menstrual cycle.

Plasma proteomic signature of the human menstrual cycle.

Journal: Nature medicine

Published: September 17, 2025

Lipoprotein(a), interleukin-6 and cardiovascular risk in a primary prevention setting.

Lipoprotein(a), interleukin-6 and cardiovascular risk in a primary prevention setting.

Journal: Atherosclerosis

Published: September 16, 2025

Genomics of chronic dry cough unravels neurological pathways.

Genomics of chronic dry cough unravels neurological pathways.

Journal: The European respiratory journal

Published: December 02, 2024

Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development.

Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development.

Journal: JHEP reports : innovation in hepatology

Published: November 29, 2024

Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndrome.

Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndrome.

Journal: European heart journal

Published: October 28, 2024

Genome-Wide Association Study of Accessory Atrioventricular Pathways.

Genome-Wide Association Study of Accessory Atrioventricular Pathways.

Journal: JAMA cardiology

Published: September 04, 2024

Genome-Wide Association Study of Plasma Sodium Concentrations with and without Exposure to Thiazide Diuretics.

Genome-Wide Association Study of Plasma Sodium Concentrations with and without Exposure to Thiazide Diuretics.

Journal: Journal of the American Society of Nephrology : JASN

Published: August 29, 2024

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Journal: American journal of human genetics

Published: August 18, 2024

Showing 1-12 of 62

Last Updated: 09/26/2026